🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Megan T. Cho

National Institutes of Health

ORCID: 0000-0001-5666-5376

Also affiliated with Johns Hopkins University, National Human Genome Research Institute

Biochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile
0Author DataRank

Indexed papers

0in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 10 papers. Top paper: “Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients”.

Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients

Science Advances(2020)10.1126/sciadv.abc9207
N/A
0DataRank · unranked
99 citations

Dong Li, Samuel G. Cox, Dylan M. Marchione, Evan F. Joiner, Khadija Wilson +95 more

A qualitative study of Latinx parents' experiences of clinical exome sequencing

Journal of Genetic Counseling(2020)10.1002/jgc4.1276
N/A
0DataRank · unranked
23 citations

Radha Sukhu, Carrie Koval, Megan T. Cho, Aileen Espinal, Katiana Rufino +4 more

Advancing the genetic counseling profession through research: Identification of priorities by the National Society of Genetic Counselors research task force

Journal of Genetic Counseling(2020)10.1002/jgc4.1330
N/A
0DataRank · unranked
14 citations

Jehannine Austin, Meghan E. Carey, Megan T. Cho, Stephanie Harris, Erin Linnenbringer +6 more

Childhood amyotrophic lateral sclerosis caused by excess sphingolipid synthesis

Nature Medicine(2021)10.1038/s41591-021-01346-1
N/A
0DataRank · unranked
153 citations

Sandra Donkervoort, Museer A. Lone, Matthew Nalls, Kenneth Gable, Sita D. Gupta +41 more

NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain

Molecular Cell(2021)10.1016/j.molcel.2021.09.020
N/A
0DataRank · unranked
57 citations

Kimberly A. Aldinger, Chi Vicky Cheng, Takae Kiyama, Mitali Dave, Hanna K. McNamara +21 more

NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain

Molecular Cell(2021)10.1016/j.molcel.2021.10.023
N/A
0DataRank · unranked
14 citations

Kimberly A. Aldinger, Chi Vicky Cheng, Takae Kiyama, Mitali Dave, Hanna K. McNamara +22 more

NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.30.437620
N/A
0DataRank · unranked
2 citations

Kimberly A. Aldinger, Chi Vicky Cheng, Takae Kiyama, Mitali Dave, Hanna K. McNamara +17 more

Phenotypic and genetic spectrum of ATP6V1A encephalopathy: a disorder of lysosomal homeostasis

Brain(2022)10.1093/brain/awac145
N/A
0DataRank · unranked
36 citations

Davide Mei, Katalin Kerti‐Szigeti, Sara Pepe, Mary Kay Koenig, Gretchen Von Allmen +48 more

Measuring quality and value in genetic counseling: The current landscape and future directions

Journal of Genetic Counseling(2022)10.1002/jgc4.1657
N/A
0DataRank · unranked
9 citations

Karen E. Wain, Julia Wynn, Megan T. Cho, Sonja Higgins, David Blaisdell +4 more

Beyond multiple choice: Clinical simulation as a rigorous and inclusive method for assessing genetic counseling competencies

Journal of Genetic Counseling(2024)10.1002/jgc4.1878
N/A
0DataRank · unranked
2 citations

Claire Rebecca Davis, Chenery Lowe, Maureen Flynn, Leila Jamal, Komal Bajaj +3 more